FAM72A c.154_156delinsTGT ;(p.A52C)

Variant ID: 1-206141447-GCA-TGT

NM_001123168.1(FAM72A):c.154_156delinsTGT;(p.A52C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Patterns and tempo of PCSK9 pseudogenizations suggest an ancient divergence in mammalian cholesterol homeostasis mechanisms.

Genetica
van Asch, Barbara B; Teixeira da Costa, Luís Filipe LF
Publication Date: 2021-02

Variant appearance in text: UGENE: A52C
PubMed Link: 33515402
Variant Present in the following documents:
  • Main text
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